List of variants reported as pathogenic for Autosomal recessive nonsyndromic hearing loss 3 by Revvity Omics, Revvity

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_016239.4(MYO15A):c.8707C>T (p.Arg2903Ter)	rs768257384	0.00001
NM_016239.4(MYO15A):c.9400C>T (p.Arg3134Ter)	rs1330631412	0.00001
NM_016239.4(MYO15A):c.373_374del (p.Arg125fs)	rs878853239
NM_016239.4(MYO15A):c.5001del (p.Gln1669fs)	rs2142326062

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